Results 21 to 30 of about 21,499 (225)

Anemia hemolítica autoimune e colite ulcerosa.

open access: yesActa Médica Portuguesa, 1995
Although several associations of autoimmune disorders with ulcerative colitis have been reported, autoimmune hemolytic anemia is extremely rare. We report a case of a 35 year-old white woman with a twelve-year history of mild ulcerative colitis treated ...
L Rebocho, M Lucas, R M Victorino
doaj   +1 more source

Problem of the diagnosis of acquired hemolytic anemia in childhood

open access: yesZdorovʹe Rebenka, 2020
Autoimmune hemolytic anemia is a heterogeneous group of diseases that are associated with decompensated acquired hemolysis. Autoimmune hemolytic anemia in children is most commonly observed after a viral illness. However, it is quite a rare disorder with
S.O. Nykytyuk   +4 more
doaj   +1 more source

CAQ Corner: Immune‐mediated complications

open access: yes, 2022
Liver Transplantation, EarlyView.
Mary Thomson, John R. Lake
wiley   +1 more source

Associations between selected immune-mediated diseases and tuberculosis: record-linkage studies. [PDF]

open access: yes, 2013
BACKGROUND: Previous studies have suggested that there may be an association between some immune-mediated diseases and risk of tuberculosis (TB). METHODS: We analyzed a database of linked statistical records of hospital admissions and death certificates ...
Michael J Goldacre   +10 more
core   +2 more sources

SEVEREULCERATIVE COLITIS ASSOCIATED WITH COOMBS POSITIVE AUTOIMMUNE HEMOLYTIC ANEMIA TREATED WITH INFLIXIMAB [PDF]

open access: yes, 2021
Autoimmune hemolytic anemia is rarely associated with ulcerative colitis, and counts only for 0.2-0.7% of adult patient.Coombs positive autoimmune hemolytic anemia which account for only 1.82% in patient with ulcerative colitis without any hemolytic ...
Busbaih , Albatool Abdulmajeed , Hodaya , Ghufran Ali , Busbaih and Jawad Salman
core   +1 more source

Severe autoimmune hemolytic anemia complicating hereditary spherocytosis treated successfully with glucocorticoids and cyclosporine: a case report

open access: yesHematology, 2023
Background Severe autoimmune hemolytic anemia complicating hereditary spherocytosis is life threatening and has not been described in a case report. Here, we report a case in which this intractable disease was treated successfully with glucocorticoids ...
Na Wang   +4 more
doaj   +1 more source

Autoimmune hemolytic anemia as an initial manifestation of Hodgkin’s Disease: Case report [PDF]

open access: yes, 2016
This paper presents the case of an 11 year-old male who attended the Internal Medicine Service at a high complexity pediatric hospital. Initially, the patient attended due to a clinical profile consisting of autoimmune hemolytic anemia that was partially
Urrego-Díaz, José Augusto   +11 more
core   +1 more source

Successful therapeutic plasma exchange in cold autoimmune hemolytic anemia in patient with disseminated tuberculosis

open access: yesReumatismo, 2021
An association of autoimmune hemolytic anemia with disseminated tuberculosis is an exceedingly rare entity. We describe herein a case of cold hemolytic autoimmune anemia associated with miliary tuberculosis resolved with blood transfusions, therapeutic ...
N. Belfeki   +7 more
doaj   +1 more source

Preleukemia: hematological disorders prior to onset of leukemia [PDF]

open access: yes, 1975
Published data on Japanese leukemia patients with a preleukemic hematological disorder were assessed. The reexamined cases were from the "Japona Centra Revuo Medicina" reported during the period from 1952 to 1971.
Mikochi, Hiroshi   +5 more
core   +1 more source

Essential thrombocythemia, hemolytic anemia and hepatic cirrhosis: Could there be an association?

open access: yesHematology Reports, 2018
Vascular events are the most common clinical complication of essential thrombocythemia, leading to sign and symptoms of this disease. There are various sign and symptoms of essential thrombocythemia, such as thrombosis in artery or vein, and enlarged ...
Nata Pratama Hardjo Lugito   +4 more
doaj   +1 more source

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